Tan Binghua, Xu Ke, Lyu Yingcheng, Liang Yicheng, Liang Ruihao, Lei Kai, Liang Jialu, Huang Jing, Wang Kefeng, Wu Duoguang, Wang Wenjian, Hu Xueting, Wang Kexi, Wang Minghui, Lin Huayue
Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Department of Thoracic Surgery, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Commun Biol. 2025 Mar 8;8(1):394. doi: 10.1038/s42003-025-07819-0.
Primary pulmonary lymphoepithelioma-like carcinoma (PPLELC) is a rare subtype of non-small-cell lung cancer. Duo to the current lack of precise targeted therapies, there is an urgent need to identify novel therapeutic targets. In this study, we perform single-nucleus transcriptome analysis on PPLELC samples to reveal the molecular tumor heterogeneity and characterize the functional states of immune cells within the tumor microenvironment. We identify a critical malignant subpopulation of PPLELC characterized by elevated expression of AKT3 and FGFR2. Higher expression levels of AKT3 and FGFR2 are associated with poorer patient outcomes. Moreover, treatment with either an AKT3 inhibitor or an FGFR2 inhibitor significantly attenuates tumor progression in patient-derived xenograft models. Our findings highlight AKT3 and FGFR2 as potential therapeutic targets and prognostic biomarkers, providing valuable insights for the development of rational targeted therapies and immunotherapeutic strategies.
原发性肺淋巴上皮瘤样癌(PPLELC)是一种罕见的非小细胞肺癌亚型。由于目前缺乏精确的靶向治疗方法,迫切需要确定新的治疗靶点。在本研究中,我们对PPLELC样本进行单核转录组分析,以揭示肿瘤分子异质性,并表征肿瘤微环境中免疫细胞的功能状态。我们鉴定出一个以AKT3和FGFR2表达升高为特征的PPLELC关键恶性亚群。AKT3和FGFR2的较高表达水平与患者较差的预后相关。此外,在患者来源的异种移植模型中,使用AKT3抑制剂或FGFR2抑制剂治疗可显著减缓肿瘤进展。我们的研究结果突出了AKT3和FGFR2作为潜在治疗靶点和预后生物标志物的作用,为合理的靶向治疗和免疫治疗策略的开发提供了有价值的见解。